Alcohols. 



470 



1230 



ALCOHOLS GuHisO 



f-Phenyl-j9-methylamyl alcohol 

 C 6 H 5 .[CH I ]3.CHMe.CH,OH 



Braun u. Kirschbaum. B„ 47, 264). 

 ALCOHOLS CuH 20 O 



Pheuyldiisopropylcarbinol 



(Me ; CIli,.Ct'h.t>ll 

 Murat tt Amoureux. Bl. [4], 15, (161). 



e-Phenyl-35-dimethylamyl alcohol 

 CH 2 Ph.CHMe.CH 2 .CHMe.CH 2 OH 



Braun u. Kirschbaum. 13., 47, (267). 



ALUOHOLS CnH : .,- s 

 ALCOHOL Ci 3 H ia 



f-Phenyl-di-s-methylpentenol 



C 6 H 5 .CH(0H).CMe 2 .0 3 H 5 



HaUer et Bauer. C.R., 158, (825). 



PHENOLS CnH 2 ..-uO 



PHENOLS CioHbO 



Naphthols. 



Hinsberg. 111848. o-Xaphtolsulfid 

 und IscH3-naphtolsulfid. 



Sen-Gupta. 115050. Condensation 

 of ketones with a-naphtbol. 



PHENOLS CnHioO 



3- Methyl- i-naphthol Me.C 10 H 6 .OH 

 Lesser. A., 402, (42). 



l-Methyl-2-naphthol. 

 Fries. 111059. Autoxydation. 



Triphenylcarbinyl ether MeC 10 H 6 O.CPhg 

 Pummerer u. Cherbuliez. B., 47, 

 (2957). 



ALCOHOLS CnH 2 ..- 12 



ALCOHOL Ci 7 H 22 



i-Naphthyl-"-hexyl-carbinol. 

 Kenyon & Pickard. 112276. The 

 rotatory power of 1-naphthyl-n-hexyl- 



carbinol and its estei - 



PHENOLS CnHjn-uO 



PHENOLS C13H12O 



2-Isopropenyl- 1 -naphthol 

 CH iCMe.C, !l„.OH 

 Preissecker. M\, 35, (889). 



£-Isopropenyl-# naphthol 



EO.C 10 H 6 .CMe : CH, 



Acetyl derivative. 



Lammer. SI., 35, (174) 



o-Oxydiphenylmethane. Methyl ether. 

 Spath. .M., 34, (1998 



ALCOHOLS C„H 2 n- 14 

 ALCOHOL C 13 Hi 2 



Benzhydrol. 



Sabatier et Murat. L14721. Pre- 

 paration du benzhydrol on du tetra- 

 phenylethane symetrique. 



ALCOHOL Cic,H 24 



2:4:5:2:4': V-Hexamethylbenz- 

 hydrol fC 6 H 2 Me 3 ) 2 CH.OH 

 Wenzel. M., 35, (987). 



ALCOHOLS CnH 2 „- 22 

 ALCOHOL CisHieO 



Triphenylcarbinol Cl'h 3 .OH 



Copisarow. 110237. Formation. 



ALCOHOLS C„H 2 n- 26 

 ALCOHOL C iH 16 



Dinaphthylcarbinol (e 10 H 7 ) 2 CH.OH 



Tschitschibabin u. Magidson. 115646. 

 Einwirkung der Phosphorsaure aui das 

 Di-o-naphtylcarbinoL 



PHENOLS CmH 2 „_4oO 

 PHENOL C 3 iH 22 



Di-aa-naphthylcarbinyl-a naphthol 



1K).C 10 H 6 .CH(C 10 H 7 ) 2 

 Acetyl derivative. 



Preissecker. M., 35, 8 19 



DIOLS. 



Remmert. 114404. Aromatische 

 Glycole. 



Simonis u. Remmert. 115118. Einige 

 fettaromatische Glykole. 



PHENOLS C,,rl\„- b 2 



PHENOLS C 6 H 6 02 



Gray & Cruikshanks. 1 1 1830. Method 

 of separating the dihydroxybenzenes. 



